FDA product code · Clinical chemistry

Menstrual Blood Collection Device

Name: FDA decisions, review times, recalls and adverse event reports for product code QZG
Creator: 510(k) Report

QZGClass II21 CFR 862.1675510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

Intended to collect and transport menstrual blood specimens to the laboratory for in vitro diagnostic testing

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, clinical chemistry panel

Twenty years of QZG at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FIG. 1 — QZG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QZG? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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